European Journal of Immunology · 2022 · 54 citations · 101 references
Life SciencesCell BiologyImmunologyCell TherapyCellular ImmunologyInnate ImmunityAnimal Cell CultureCell CharacterizationCell Source SelectionDendritic Cell BiologyImmune Cell DifferentiationInnate Immune Cell DevelopmentCrispr-cas9 Ex Vivo EditingCrispr-cas9 Genome EditingCrispr-cas9 KnockoutDendritic Cell EngineeringDendritic Cell Subset SpecificationFlow Cytometry ImmunophenotypingGene-modified Dendritic CellsImmune Cell Sources
Abstract This article is part of the Dendritic Cell Guidelines article series, which provides a collection of state‐of‐the‐art protocols for the preparation, phenotype analysis by flow cytometry, generation, fluorescence microscopy, and functional characterization of mouse and human dendritic cells (DC) from lymphoid organs and various non‐lymphoid tissues. This article provides protocols with top ticks and pitfalls for preparation and successful generation of mouse and human DC from different cellular sources, such as murine BM and HoxB8 cells, as well as human CD34 + cells from cord blood, BM, and peripheral blood or peripheral blood monocytes. We describe murine cDC1, cDC2, and pDC generation with Flt3L and the generation of BM‐derived DC with GM‐CSF. Protocols for human DC generation focus on CD34 + cell culture on OP9 cell layers for cDC1, cDC2, cDC3, and pDC subset generation and DC generation from peripheral blood monocytes (MoDC). Additional protocols include enrichment of murine DC subsets, CRISPR/Cas9 editing, and clinical grade human DC generation. While all protocols were written by experienced scientists who routinely use them in their work, this article was also peer‐reviewed by leading experts and approved by all co‐authors, making it an essential resource for basic and clinical DC immunologists.
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